Title of article
Regioselective Michael-induced cyclisation of γ- and δ-hydroxy vinyl sulfides and vinyl dithiocarbamates
Author/Authors
Vincent Aucagne، نويسنده , , V. and Lorin، نويسنده , , C. and Tatibouët، نويسنده , , A. and Rollin، نويسنده , , P.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
4
From page
4349
To page
4352
Abstract
We herein describe the unprecedented use of heteroaryl vinyl sulfides and vinyl dithiocarbamates as hetero-Michael addition acceptors. Combined chelating and electron-withdrawing effects are postulated to stabilise the transient anionic species and allow smooth Michael-induced ring closure to produce diversely functionalised C-glycosides.
Keywords
Vinyl sulfides , Hetero-Michael additions , Vinyl dithiocarbamates , C-Glycosides
Journal title
Tetrahedron Letters
Serial Year
2005
Journal title
Tetrahedron Letters
Record number
1845982
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